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Updated: Aug 27, 2025

Hydrolysis of a Ni-Schiff-Base Complex Using Conditions Suitable for Retention of Acid-labile Protecting Groups
Published on: April 6, 2017
Architectural MCM 41 was anchored to the Schiff base Co(II) complex to enhance methylene blue dye degradation and
Manikandan Palaniappan1, David Selvaraj2, Sabariswaran Kandasamy3
1Department of Chemistry, Bioinorganic Lab, Science Block-1, Periyar University, Salem 636 011, Tamil Nadu, India.
Abstract:
A sequence of Schiff base Cobalt (II) Mobile Composite Matter 41 heterojunction (SBCo(II)-MCM 41) was prepared by post-synthetic protocols. Various characterization techniques were used to characterize the above samples and MCM 41: Morphology, functional groups, optical properties, crystalline nature, pore diameter, and binding energy by scanning electron microscope (SEM), High-resolution transition electron microscopy (HR-TEM), Fourier transform infrared spectroscopy (FTIR), Ultra Violet-Visible Spectroscopy (UV), X-ray powder diffraction (XRD), Brunauer-Emmett-Teller (BET) and X-ray Photoelectron Spectroscopy (XPS). After the encapsulation of SBCo(II) on the MCM 41, the intensity in the 100-plane in powder x-ray diffraction (XRD) decreased significantly; moreover, the light absorption behavior in UV analysis was improved. The change in the surface area and the decrease in the pore diameter of the sample were also demonstrated by the BET study. The XPS results confirmed the presence of Si, O, C, N, and Co in the SBCo(II)-MCM 41 complex. The photocatalytic performance of MCM 41 and SBCo(II)-MCM 41 materials tested by the degradation of methylene blue dye (MBD) shows that MCM 41 immobilization with SBCo(II)complex is rapidly degraded under natural sunlight irradiation. The optimized 10 mg SBCo(II)-MCM 41 catalyst concentrations showed effective enhancement with the highest efficiency of 98% achieved within 2 h compared to the other two SBCo(II)-MCM 41 concentrations. Moreover, the catalytic efficiency of SBCo(II)-MCM 41 showed a biomimetic reaction without using an oxidant, which exposed it as an effective catalyst for amine to imine conversion; it was useful in the medical field for enzymes with structural assembly.
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